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rs121918397

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918397(A;A)
Make rs121918397(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44908784
GeneAPOE
is asnp
is mentioned by
dbSNPrs121918397
ebirs121918397
HLIrs121918397
Exacrs121918397
Varsomers121918397
Maprs121918397
PheGenIrs121918397
hapmaprs121918397
1000 genomesrs121918397
hgdprs121918397
ensemblrs121918397
gopubmedrs121918397
geneviewrs121918397
scholarrs121918397
googlers121918397
pharmgkbrs121918397
gwascentralrs121918397
openSNPrs121918397
23andMers121918397
23andMe allrs121918397
SNP Nexus

SNPshotrs121918397
SNPdbers121918397
MSV3drs121918397
GWAS Ctlgrs121918397
Max Magnitude0
OMIM107741
Desc
Variant0018
Relatedalso
OMIM107741
Desc
Variant0032
Relatedalso
ClinVar
Risk rs121918397(A,C;A,C)
Alt rs121918397(A,C;A,C)
Reference rs121918397(G;G)
Significance Pathogenic
Disease Familial type 3 hyperlipoproteinemia APOE3(-)-KOCHI Lipoprotein glomerulopathy APOE SENDAI
Variation info
Gene APOE
CLNDBN Familial type 3 hyperlipoproteinemia APOE3(-)-KOCHI Lipoprotein glomerulopathy APOE SENDAI
Reversed 0
HGVS NC_000019.9:g.45412041G>A; NC_000019.9:g.45412041G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019449.28, RCV000019450.28, RCV000019466.24, RCV000019467.28,